In this study, the allelopathic properties of Medicago sativa on different weeds were investigated under in vitro conditions. The compounds involved in the autotoxicity of M. sativa were analyzed using high-performance liquid chromatography. The extracts of all concentrations inhibited the growth of the calluses of Digitaria ciliaris, Chenopodium album, Amaranthus lividus, Portulaca oleracea, and Commelina communis. Six allelopathic compounds in alfalfa were identified and quantified, and the most predominant phenolic compounds were salicylic acid and p-hydroxybenzoic acid. Various concentrations (10−2, 10−3, and 10−5 M) of all the tested phenolic compounds exerted inhibitory effects on callus fresh weight. Rutin, salicylic acid, scopoletin, and quercetin significantly inhibited alfalfa seed germination. Of the seven identified saponins, medicagenic acid saponins exhibited the highest autotoxic effect and significantly lowered seed germination rate. Principal component analysis showed that the phenolic compounds and saponin composition significantly contributed to the different variables. The highly phytotoxic properties of the alfalfa-derived phenolic compounds and saponins indicate that these phytochemicals can be a potential source of bioherbicides.
We studied the elevational pattern of forest composition and regeneration of the subalpine conifer tree species Pinus wallichiana in Manang, a trans-Himalayan dry valley in north-central Nepal. Thirty-five quadrats (10 m × 10 m) were laid between 3300 and 4000 masl on both north-and south-facing slopes. We measured diameter at breast height (DBH) of each mature individual of all tree species (DBH ≥10 cm), and recorded the number of seedlings (DBH <10 cm, height <30 cm) and saplings (DBH <10 cm, height >30 cm). We also measured soil moisture and soil pH, estimated canopy cover, and recorded slope and altitude in each quadrat. For all species together and for several species individually, tree density, seedling density, sapling density and tree basal area were found to decrease with elevation on both north and south aspects. This trend is largely explained by the progressively harsher environment at higher elevations. The north-facing slopes in our study area have denser forests than the south-facing slopes, the density of all size classes (seedling, sapling and mature plants) and basal area being greater on the northern aspects. These aspect-wide differences are attributable to the stark difference in soil moisture between northern and southern aspects, which is in turn due to the difference in insolation. Irrespective of elevation and aspect, all the forests studied are regenerating, as indicated by inverse J-shaped density-diameter curves. The elevational pattern of seedling and sapling abundance is explained only by elevation. Whereas other variables (e.g., canopy) are considered to have an important influence on seed germination and seedling establishment, they turn out not to be significant predictors of density of seedlings and saplings. This failure to identify a relationship is probably due to our use of non-parametric test (tree regression analysis) that we used to establish the relationship between density and its potential explanatory variables or due to our selection of 1 standard error rule yielding sub-optimal models for regression trees.
The comparative study on leaf anatomy and stomata structures of six genera of Taxaceae s. l. was conducted. Leaf anatomical structures were very comparable to each other in tissue shape and their arrangements. Taxus, Austrotaxus, and Pseudotaxus have no foliar resin canal, whereas Amentotaxus, Cephalotaxus, and Torreya have a single resin canal located below the vascular bundle. Among them, Torreya was unique with thick-walled, almost round sclerenchymatous epidermal cells. In addition, Amentotaxus and Torreya were comprised of some fiber cells around the vascular bundle. Also, Amentotaxus resembled Cephalotaxus harringtonia and its var. nana because they have discontinuous fibrous hypodermis. However, C. fortunei lacked the same kind of cells. Stomata were arranged in two stomatal bands separated by a mid-vein. The most unique stomatal structure was of Taxus with papillose accessory cells forming stomatal apparatus and of Torreya with deeply seated stomata covered with a special filament structure. Some morphological and molecular studies have already been discussed for the alternative classification of taxad genera into different minor families. The present study is also similar to these hypotheses because each genus has their own individuality in anatomical structure and stomata morphology. In conclusion, these differences in leaf and stomata morphology neither strongly support the two tribes in Taxaceae nor fairly recognize the monogeneric family, Cephalotaxaceae. Rather, it might support an alternative classification of taxad genera in different minor families or a single family Taxaceae including Cephalotaxus. In this study, we would prefer the latter one because there is no clear reason to separate Cephalotaxus from the rest genera of Taxaceae. Therefore, Taxaceae should be redefined with broad circumscriptions including Cephalotaxus.
A number of conifer species are still lacking anatomical data, which is significant because morphological and anatomical data are essential for systematic study. Leaf anatomy was studied in selected species of Abies and Picea using light and scanning electron microscopy. Both genera were found to have typical coniferous and highly xerophytic leaves with sunken stomata and an epidermis covered by a thick cuticle. In the genus Abies, species can be differentiated by the nature of the lignified hypodermis and the number and position of resin ducts. Abies firma and A. holophylla have a continuous hypodermis whereas in A. koreana and A. nephrolepis the hypodermis is discontinuous and represented by isolated cells or groups of four or five cells. On the other hand, in Picea leaf shape, stomata arrangement, and number, position, and nature of resin ducts are the key features for species differentiation. Picea jezoensis has a flattened leaf with stomata distributed on the adaxial surface whereas P. abies and P. koraiensis have a rectangular leaf with stomata found on surfaces.
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